Emg CTA01-XXX Series Puro Oxygen Concentrator
FDA 510(k) K043520 · Emg Technology Co., Ltd.
510(k) numberK043520
Submission
- Device name
- Emg CTA01-XXX Series Puro Oxygen Concentrator
- Applicant
- Emg Technology Co., Ltd.
Baltimore, MD, US - Received
- December 20, 2004
- Decision date
- October 21, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Abbreviated 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- CAW – Generator, Oxygen, Portable
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5440
- Specialty
- Anesthesiology
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| K252399 | Portable Oxygen ConcentratorCAW · Traditional | Honsun (Nantong) Co., Ltd. | 06/17/2026SE |
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| K253549 | DeVilbiss 5 Liter Oxygen Concentrator (555)CAW · Traditional | Devilbiss Healthcare, LLC | 03/26/2026SE |
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| K252616 | Portable oxygen concentrator (JLO-190P)CAW · Traditional | Shenzhen Homed Medical Device Co., Ltd. | 12/22/2025SE |
| K251764 | Oxygen Concentrator-P2-O5ECAW · Traditional | Qingdao Kingon Medical Science and Technology… | 12/22/2025SE |
| K252268 | V series portable oxygen concentrator (V5, V5C, V6, V6C)CAW · Traditional | Shenzhen Harveymed Technology Co., Ltd. | 12/16/2025SE |
| K250805 | DeVilbiss PulmO2 10-Liter Oxygen Concentrator (1060AW)CAW · Traditional | Devilbiss Healthcare, LLC | 12/09/2025SE |
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Questions and answers
When was Emg CTA01-XXX Series Puro Oxygen Concentrator cleared by the FDA?
Emg CTA01-XXX Series Puro Oxygen Concentrator (K043520) received a 510(k) decision of Substantially Equivalent on October 21, 2005, 305 days after the submission was received.
What is the product code of K043520?
The FDA product code is CAW – Generator, Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5440.